• Polymer Chemist

    Kelly Services (Raritan, NJ)
    …with Polymer Process Engineers to optimize process parameters for large-scale manufacturing . The ideal candidate will possess a solid background in polymer ... with Polymer Process Engineers to optimize parameters for larger-scale manufacturing . + Documentation and Reporting: Maintain accurate records of experimental… more
    Kelly Services (07/26/25)
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  • Quality Control Inspector I - 1st shift

    Integra LifeSciences (Plainsboro, NJ)
    …appropriate test records. * Perform line clearances and quality reviews in manufacturing , labeling, or other assigned areas during manufacturing activities. * ... specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. * QA experience in the medical device… more
    Integra LifeSciences (07/24/25)
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  • Validation Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …and launching of new equipment or products and processes into a manufacturing facility. The candidate must utilize problem solving techniques to resolve issues ... Validation or Quality Assurance role for a medical device or pharmaceutical environment. + Demonstrates excellent organizational and communication skills. +… more
    Integra LifeSciences (07/22/25)
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  • Director, Clinical Logistics Global Capability…

    Bristol Myers Squibb (New Brunswick, NJ)
    …years of experience in digital or data technology, operations, supply chain, manufacturing , ERP, clinical supply chain, logistics preferably in the pharmaceutical ... of relevant Quality compliance processes and regulations, eg Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), Good Distribution Practices… more
    Bristol Myers Squibb (07/16/25)
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  • Global Director, Continuous Improvement

    Catalent Pharma Solutions (Bridgewater, NJ)
    …years' experience in Operations and Continuous Improvement roles in complex manufacturing environments, strongly prefer a biologics, pharma technical and product ... working to regulatory standards: FDA, Good Engineering Practice (GEP), Good Manufacturing Procedures (GMP) and Good Documentation Procedures (GDP). + Demonstrated… more
    Catalent Pharma Solutions (07/08/25)
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  • Quality Control Inspector I, 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …appropriate test records. + Perform line clearances and quality reviews in manufacturing , labeling, or other assigned areas during manufacturing activities. + ... specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device… more
    Integra LifeSciences (06/16/25)
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  • Global Marketing Manager - BD Vacutainer Tubes

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the ... + At least 3 to 5+ years' work experience (IVD, Medical Device, Pharmaceutical or consulting experience is preferred) + Business experience may include marketing,… more
    BD (Becton, Dickinson and Company) (08/30/25)
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  • Manager, Tax Operations

    Bristol Myers Squibb (Madison, NJ)
    …preferably 2+ years of public accounting experience working in a complex manufacturing environment, preferable in the pharmaceutical industry. + In-depth ... knowledge of tax laws, regulations, and accounting principles, including GAAP and Non-GAAP accounting, legal entity forecasting and accounting. + Solid technology background with knowledge of OneSource Provision (knowledge of TaxStream is very beneficial),… more
    Bristol Myers Squibb (08/30/25)
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  • Innovative Medicine Transcend (ERP) Program…

    J&J Family of Companies (Titusville, NJ)
    …10 years of progressive experience with GxP regulated processes in the pharmaceutical industry, preferably Quality Assurance, Supply Chain, Manufacturing or HSE ... (Health, Safety & Environment). + Hands-on experience of applying Business Quality (GXP) in an ERP setting, preferably using Agile methodology. + Required experience of applying SDLC principles in an ERP setting. + Minimum 5 years of hands-on expeperience… more
    J&J Family of Companies (08/30/25)
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  • CSV Technical Writer

    Capgemini (Titusville, NJ)
    …+ Collaborate with cross-functional teams including Quality, Engineering, Regulatory, and Manufacturing to gather source material and ensure accuracy + Translate ... bring:** + 3-5+ years of experience as a Technical Writer in the pharmaceutical or life sciences industry + Strong understanding of validation processes (equipment,… more
    Capgemini (08/30/25)
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